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奥美拉唑在母羊和胎羊体内的胎盘转运。

Placental transfer of omeprazole in maternal and fetal sheep.

作者信息

Ching M S, Morgan D J, Mihaly G W, Hardy K J, Smallwood R A

出版信息

Dev Pharmacol Ther. 1986;9(5):323-31. doi: 10.1159/000457111.

Abstract

The placental transfer of omeprazole was studied over a 4-fold dose range in 7 nonanesthetized near-term pregnant sheep. There was a 5 to 1 maternal to fetal transplacental gradient of steady-state total omeprazole concentrations after both low dose (maternal plasma 556 +/- 361 ng/ml, fetal plasma 101 +/- 57 ng/ml) and high dose (maternal plasma 2,660 +/- 1,130 ng/ml, fetal plasma 563 +/- 182 ng/ml). Although this was in part due to differences in plasma protein binding between mother (unbound fraction 6.6 +/- 5.5%) and fetus (unbound fraction 11.9 +/- 2.4%), a 2 to 1 maternal to fetal gradient of steady-state unbound omeprazole concentration was still present (144 +/- 73 ng/ml vs. 64 +/- 32 ng/ml). Fetal omeprazole total plasma concentrations correlated strongly with maternal total drug concentrations (r = 0.84, p less than 0.025) and with the inverse of maternal omeprazole total systemic clearance (r = 0.77, p less than 0.05), indicating that maternal drug disposition was a major determinant of fetal omeprazole plasma concentrations. Urinary clearance of omeprazole was low in both mother (0.137 +/- 0.046 ml/min) and fetus (0.067 +/- 0.039 ml/min). This study demonstrates that the fetus is exposed to about one half of the unbound omeprazole concentration in maternal plasma and suggests that the extent of fetal exposure is largely dictated by maternal drug distribution and elimination characteristics.

摘要

在7只未麻醉的近足月妊娠绵羊中,研究了4倍剂量范围内奥美拉唑的胎盘转运情况。低剂量(母体血浆556±361 ng/ml,胎儿血浆101±57 ng/ml)和高剂量(母体血浆2660±1130 ng/ml,胎儿血浆563±182 ng/ml)给药后,稳态时奥美拉唑总浓度的母胎胎盘梯度为5比1。虽然这部分归因于母体(未结合分数6.6±5.5%)和胎儿(未结合分数11.9±2.4%)血浆蛋白结合的差异,但稳态时未结合奥美拉唑浓度仍存在2比1的母胎梯度(144±73 ng/ml对64±32 ng/ml)。胎儿奥美拉唑总血浆浓度与母体总药物浓度密切相关(r = 0.84,p<0.025),与母体奥美拉唑总全身清除率的倒数密切相关(r = 0.77,p<0.05),表明母体药物处置是胎儿奥美拉唑血浆浓度的主要决定因素。母体(0.137±0.046 ml/min)和胎儿(0.0�7±0.039 ml/min)的奥美拉唑尿清除率均较低。本研究表明,胎儿暴露于母体血浆中约一半的未结合奥美拉唑浓度,提示胎儿暴露程度很大程度上由母体药物分布和消除特征决定。

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